Retrospective Comparison between 12-Gray and 8-Gray Total Body Irradiation (TBI) before Allogeneic Hematopoietic Cell Transplantation in Patients with Acute Lymphoblastic Leukemia in First Complete Remission

Introduction: Total body irradiation (TBI) continues to be an important part of the conditioning regimen for allogeneic hematopoietic cell transplantation (allo-HCT) in acute lymphoblastic leukemia (ALL). Previous dose escalation studies showed that higher than 12-Gray (Gy) was toxic and did not pro...

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Veröffentlicht in:Blood 2021-11, Vol.138 (Supplement 1), p.1783-1783
Hauptverfasser: Spyridonidis, Alexandros, Labopin, Myriam, Savani, Bipin B., Giebel, Sebastian, Schmid, Christoph, Peric, Zinaida, Bug, Gesine, Schönland, Stefan, Kröger, Nicolaus, Stelljes, Matthias, Schroeder, Thomas, McDonald, Andrew, Blau, Igor Wolfgang, Bornhäuser, Martin, Rovira, Montserrat, Bethge, Wolfgang, Neubauer, Andreas, Ganser, Arnold, Bourhis, Jean-Henri, Edinger, Matthias, Lioure, Bruno, Wulf, Gerald, Schaefer-Eckart, Kerstin, Arat, Mutlu, Bazarbachi, Ali, Nagler, Arnon, Mohty, Mohamad
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Sprache:eng
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Zusammenfassung:Introduction: Total body irradiation (TBI) continues to be an important part of the conditioning regimen for allogeneic hematopoietic cell transplantation (allo-HCT) in acute lymphoblastic leukemia (ALL). Previous dose escalation studies showed that higher than 12-Gray (Gy) was toxic and did not provide any apparent survival benefit - at least in patients (pts) transplanted in first complete remission (CR1) - thus establishing 12-Gy as the standard TBI dosage. Whether 8-Gy instead of 12-Gy TBI is sufficient in ALL CR1, as has been prospectively demonstrated for AML CR1 (Lancet Oncol 2012; 13: 1035-1044), has not yet been studied. Methods: In this registry-based retrospective study of the Acute Leukemia Working Party of the European Society for Blood and Marrow Transplantation (ALWP-EBMT), we compared outcomes of ALL-CR1 pts who underwent a matched-sibling donor (MSD) or matched-unrelated donor (MUD) allo-HCT (94% peripheral blood stem cells) with TBI-based conditioning at a total dose of 12-Gy vs 8-Gy. Patients included in this analysis had received fludarabine (Flu) as the sole chemotherapy counterpart of TBI (12-Gy vs 8-Gy TBIFlu). Results: The median follow up for the whole cohort (n=639 pts) was 22.5 months (95% CI, 17.2-24.1) and did not differ between the 8-Gy (n=494) and 12-Gy (n= 145) TBIFlu treated pts. 25% pts had B-precursor ALL, 54% Philadelphia (Ph)-positive ALL and 21% T-ALL (p=0.008 between groups). Patients conditioned with 8-Gy TBIFlu were older than 12-Gy TBIFlu treated pts (median 55.7 vs 40.3 years, IQR 50.2-61.3 vs 27-50.2 years,
ISSN:0006-4971
1528-0020
DOI:10.1182/blood-2021-145100